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Quality Management

Materials for clinical trials must be fit for their intended use

Pharmaceutical products including materials for clinical trials must be fit for their intended use, comply with the relevant requirements and must not place patients at risk due to inadequate safety, quality or efficacy.

To achieve this quality objective in a reliable manner, the team at ABF has implemented a comprehensive quality management system in which all quality assurance measures are based on Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP).

ABF Manufacturer’s Authorisation 2015 / ABF GMP Certificate 2015

  • Comprehensive QM System
  • GMP, GCP and ICH Implemented

We operate to the highest of audited quality standards.

Your direct contact

Benjamin Baranyai
Senior Business Development Manager
+43 676 897 11 55 20
Benjamin.Baranyai@abf-pharma.com

Business Development

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To learn more about us and what we can do for you please contact our Senior Business Development Manager.

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Our experienced and committed team offers a comprehensive range of services in the following areas

Labeling & Packaging

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Storage

Import & Export

QP Release

PBMC

Sourcing

Clinical Trial Supply

GBA Group Pharma

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